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FAM58A gene

Known as: FAM58A, MGC29729, FLJ21610 
 
National Institutes of Health

Related topics

Related topics

1 relation
GAREM1 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Detection of copy number variation and selection signatures on the X chromosome in Chinese indigenous sheep with different types of tail
Objective Chinese indigenous sheep breeds can be classified into the following three categories by their tail morphology: fat… Expand
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Review
2017
Review
2017
The awakening of the CDK10/Cyclin M protein kinase
Cyclin-dependent kinases (CDKs) play important roles in the control of fundamental cellular processes. Some of the most… Expand
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2017
2017
Multigenerational pedigree with STAR syndrome: A novel FAM58A variant and expansion of the phenotype
STAR syndrome is a rare X‐linked dominant disorder characterized by toe Syndactyly, Telecanthus, Anogenital malformations, and… Expand
2016
2016
STAR syndrome-associated CDK10/Cyclin M regulates actin network architecture and ciliogenesis
ABSTRACT CDK10/CycM is a protein kinase deficient in STAR (toe Syndactyly, Telecanthus and Anogenital and Renal malformations… Expand
2008
2008
Mutations in the cyclin family member FAM58A cause an X-linked dominant disorder characterized by syndactyly, telecanthus and anogenital and renal malformations
We identified four girls with a consistent constellation of facial dysmorphism and malformations previously reported in a single… Expand
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